Top 23 Research coordinator Jobs in Manassas, Va

Clinical Research Nurse Coordinator I
MedStar Health —McLean, VA
- $89,065 - $162,801 a year
- Full-time
- Background check
- Nursing
- OSHA
Quick Apply
Clinical Research Coordinator
DelRicht Research —Vienna, VA
- $55,000 - $60,000 a year
- Full-time
- Bachelor of Science
- Clinic
- In-person
- Profit sharing
- Disability insurance
14d
Project Coordinator-AI-Enabled Research and Pedagogical Innovation
Northern VA Community College —Fairfax County, VA
- $35 an hour
- Part-time
- Background check
- Google Workspace
- Mid-level
- Paid parental leave
- Health insurance
4d
Research Admin Coordinator
Virginia Cancer Specialists —Fairfax, VA
- Full-time
- Mid-level
- Office
- High school diploma or GED
- Paid holidays
- Health insurance
10d
Clincal Research Coordinator II/III
ARIZONA ARTHRITIS & RHEUMATOLOGY ASSOCIATES PC —Fairfax, VA
- $67,000 - $82,744 a year
- Full-time
- Mid-level
- Office
- Bachelor's degree
Quick Apply
Clinical Research Coordinator - Urology
The Specialty Alliance —Fairfax, VA
- Full-time
- Private practice
- Blood sampling
- Writing skills
Quick Apply
Clinical Research Coordinator II
The Specialty Alliance —Fairfax, VA
- Full-time
- Management
- Patient monitoring
- HIPAA
Quick Apply
Project Coordinator-AI-Enabled Research and Pedagogical Innovation
Northern Virginia Community College —Fairfax County, VA
- $35 an hour
- Part-time
- Background check
- Google Workspace
- Mid-level
- Paid parental leave
- Health insurance
4d
Clinical Research Coordinator
Guidehouse Digital, LLC —Bethesda, MD
- $65,000 - $108,000 a year
- Full-time
- Nursing
- Mid-level
- Bachelor's degree
- Commuter assistance
- Health savings account
6d
Research Coordinator
CRDF Global —Arlington, VA
- Full-time
- Microsoft Outlook
- 5 years
- English
Scientific Working Groups and Committees (SWC) Coordinator - ON-CALL
ICF —Fairfax, VA
- $55,665 - $94,631 a year
- Part-time
- Microsoft Outlook
- Mid-level
- Bachelor's degree
Clinical Research Coordinator - National Harbor, MD
Advanced Dermatology and Cosmetic Surgery —Oxon Hill, MD
- Full-time
- Vital signs
- Basic math
- HIPAA
- 401(k)
Quick Apply
6d
Clinical Research Coordinator
Georgetown University —Washington, DC
- $44,022.00 - $73,406.80 a year
- Full-time
- Mid-level
- 3 years
- University
- Disability insurance
- Health insurance
4d
Research Data Coordinator 2
Georgetown University —Washington, DC
- $18.40 - $27.33 an hour
- Full-time
- 5 years
- HIPAA
- Mid-level
- Disability insurance
- Health insurance
6d
City Policy Coordinator
Institute for Justice —Arlington, VA
- $60,000 - $65,000 a year
- Full-time
- Hybrid work
- Mid-level
- Office
- Travel
- Health savings account
- Paid holidays
13d
Program Coordinator
BLN24 —McLean, VA
- Full-time
- 6 years
- Master's degree
- Bachelor's degree
- Dental insurance
- Vision insurance

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Clinical Research Nurse Coordinator I

MedStar Health -
McLean, VA

Quick Apply

Job Details

Full-time
$89,065 - $162,801 a year

Qualifications

RN License
Associate's degree
Associate Degree in Nursing

Full Job Description

About this Job: General Summary of Position
Under the direction of the Principal Investigator (PI) and within the scope of nursing practice the competent Clinical Research Nurse Coordinator I (CRNC I) with moderate supervision assesses plans and implements and evaluates the nursing care of potential research participants from pre-screening through study exit. Position functions under the direction of an experienced nurse to provide patient care relevant to the protocol while using professional judgment and sound decision making. The CRNC I demonstrates professional accountability and responsibility for nursing practice and coordinates care delivery with the principal investigator and other members of the clinical research teams and family. Gains perspective from planning own actions based on conscious abstract and analytical thinking and helps to achieve greater efficiency and organization. The CRNC I is responsible for the implementation of their assigned portfolio of studies which may include but not limited to IRB applications and related forms data collection forms patient screening and enrollment verification of investigative procedures to accomplish research goals and preparation of reports.

Primary Duties and Responsibilities

Contributes to the achievement of established department goals and objectives and adheres to department policies procedures quality standards and safety standards. Complies with governmental and accreditation regulations.
Consistently demonstrates support for compliance in the performance of job duties and responsibilities by a) developing and maintaining knowledge of and performing job functions in compliance with rules regulations policies and statutes that affect his/her job; b) maintaining knowledge of and performing job functions in compliance with MedStar Health and MedStar Health Research Institute policies and procedures; and c) reporting compliance concerns in an appropriate and timely manner.
Performs skills and duties that are within the scope of nursing practice with the ability to write orders with physician co-signature in the patient medical record (MedConnect). Incorporates the nursing process into holistic research participant care including clinical assessment to identify needs and problems experienced by participants and their caregivers.
Facilitates site qualification study initiation and monitoring visits; works effectively with multidisciplinary ancillary and inter-professional research teams; possesses a basic understanding of scientific center goals and the importance of serving our customers. Participates in all audits and inspections and maintains the site in an audit-ready status.
Assists and/or is responsible for the Institutional Review Board (IRB) submissions and other related regulatory forms; coordinates essential regulatory documents and submits timely and accurate regulatory documents to the Sponsor as applicable.
Pre-screens potential research participants to determine initial eligibility and interest in a research study and adheres to guidelines to protect Protected Health Information (PHI).
Conducts the research participant informed consent process according to MHRI consent policies and procedures and Good Clinical Practice. Ensures that the participant and family understand plan of care and health status implications and act as an advocate in meeting participant and family needs related to research protocol.
Collects data pertinent to the research protocol requirements and the research participant's health and/or situation. Assists the clinician/investigator in ensuring adequate source documentation and data-collection that validate the integrity of the clinical trial/research study. Documents participant encounters are updated as appropriate and within one (1) business day in a recognized electronic system/database (e.g. OnCore Clinical Trial Management System [CTMS]); enters data into various auditable databases or electronic data capture systems (e.g. REDCap).
Implements the identified healthcare and research plans communicates effectively to all study personnel employs strategies to promote health and a safe environment and practices ethically and in a manner that is congruent with inclusion principles.
Completes study required assessments using interview observation and physical examination (as appropriate) of participants consented for participation in research.
Administers or provides oversight of administration of investigational product and other treatment agents or study interventions as appropriate.
Maintains current Occupational Safety and Health Administration (OSHA) training regarding bloodborne pathogens; maintains International Air and Transportation Association (IATA) training for routine packaging labeling and transporting of biological materials to ensure proper collection processing and shipment of biospecimens as needed.
Receives and inventories test articles (study device or drug); works with research pharmacist as applicable; stores test articles according to Food and Drug Administration (FDA) regulations and Sponsor requirements; with oversight administers test articles; retrieves test articles and calculates research participant compliance as applicable; reconciles accountability log and completes research participant record.
Understands and complies with rules for billing Medicare Medicaid and third-party payors for services drugs devices tests and procedures rendered in the clinical research context; responsible for following the billing matrix/billing plan generated by administration for research participants enrolled in clinical studies; ensures research participant stipend information is submitted.
Optimizes the safety of research participants by answering participant questions regarding specific dose and side effects regarding investigational product and assess adverse events. Informs investigator of adverse events and documents seriousness causality and intervention; acts on investigator's recommendation for adverse event intervention (e.g. stop test article call research participant re-test treat); maintains follow-up to determine resolution of adverse event. Report all serious ADE's to the principal investigator sponsor primary care physician (as applicable) and IRB as outlined in the protocol.
Coordinates study close-out activities. Oversees the return disposal and/or destruction of unused supplies per Sponsor requirements; reconciles test article accountability; documents research participants who are lost to follow-up or who withdraw consent; assists in the preparation for a potential routine pre-market approval (PMA) FDA inspection as applicable.
Must comply with international federal state Sponsor and MHRI policies; must possess basic understanding of the ethical treatment of research participants and of Good Clinical Practices (GCPs) aspects of human protection and safety in the conduct of clinical research (21 CFR 50 Protection of Human Subjects 21 CFR 54 Financial Disclosure 21 C FR 56 Institutional Review Boards). Maintains required MHRI trainings including but not limited to Collaborative Intuitional Training Initiative (CITI) Conflict of Interest (COI) and annual MedStar Health mandatories.
Participates in multi-disciplinary quality and service improvement teams.

Minimal Qualifications
Education

Associate's degree in Nursing required and
Bachelor's degree of Science in Nursing preferred

Experience

1-2 years Experience of clinical practice or minimum 1 year of research experience. required

Licenses and Certifications

RN - Registered Nurse - State Licensure and/or Compact State Licensure Registered Nurse license in the state you are practicing with the ability to get reciprocity if needed. required

Knowledge Skills and Abilities

Verbal and written communication skills.
Basic computer skills preferred.

This position has a hiring range of : USD $89,065.00 - USD $162,801.00 /Yr.

Work Location: In person

Quick Apply

Refine Your Search

research coordinator jobs in manassas, va

Clinical Research Nurse Coordinator I

Clinical Research Coordinator

Project Coordinator-AI-Enabled Research and Pedagogical Innovation

Research Admin Coordinator

Clincal Research Coordinator II/III

Clinical Research Coordinator - Urology

Clinical Research Coordinator II

Project Coordinator-AI-Enabled Research and Pedagogical Innovation

Clinical Research Coordinator

Research Coordinator

Scientific Working Groups and Committees (SWC) Coordinator - ON-CALL

Clinical Research Coordinator - National Harbor, MD

Clinical Research Coordinator

Research Data Coordinator 2

City Policy Coordinator

Program Coordinator

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